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Reagents delivery

Reagent delivery It is possible to add reagents to the sample while the experiment is running using the APTAC instrument. Sample venting The pressure in APTAC s sample eontainer ean be automatieally released and the material eolleeted into an external vessel. [Pg.933]

S. Luo and D. R. Walt, Fiber-optic sensors based on reagent delivery with controlled-release polymers. Anal. Chem, 61, 174-177 (1989). [Pg.220]

Figure 5.8 — Probe-type sensor based on continuous circulation of a stream containing an acid-base indicator for the batch determination of COj in sea water, (a) Reagent delivery capillary, (d) Reagent exit capillary, (c) Optical fibre from source, (d) Optical fibre to detector, (e) White silicone rubber membrane. (/) White silicone sealant, (g) Epoxy resin, (/i) 0-ring. (/) Sensor housing. (/) Optical cable. (Reproduced from [12] with permission of the American Chemical Society). Figure 5.8 — Probe-type sensor based on continuous circulation of a stream containing an acid-base indicator for the batch determination of COj in sea water, (a) Reagent delivery capillary, (d) Reagent exit capillary, (c) Optical fibre from source, (d) Optical fibre to detector, (e) White silicone rubber membrane. (/) White silicone sealant, (g) Epoxy resin, (/i) 0-ring. (/) Sensor housing. (/) Optical cable. (Reproduced from [12] with permission of the American Chemical Society).
C. Yi and M. Gratzl, Diffusional Mictrotitration Reagent Delivery by a Diffusional Microburet into Microscopic Samples, Anal. Chem. 1994, 66, 1976 ... [Pg.670]

Enzymatic techniques have also been employed in the analysis of these compounds. The toxicity of carbamate insecticides is due to the inhibition of the enzyme acetylcholine esterase, so the determination of these compounds can be achieved by enzyme inhibition (2,83,119), bioassay (118,167), or enzyme-linked immunosorbent assay (ELISA) (168-171). In the detection of carbamates by fluorimetric enzyme inhibition, the effluent from a reversed-phase chromatographic column was incubated with cholinesterase, which was introduced via a postcolumn reagent delivery pump. Then, the resulting partially inhibited cholinesterase was reacted with N-methyl indoyl acetate to produce a fluorophore and a reduction in the baseline fluorescence (172). [Pg.706]

Cellular studies are facilitated in the microfluidic chips because of their small dimensions. In addition, the chip provides excellent optical properties for observation and flexible fluidic control capabilities for reagent delivery. [Pg.251]

Vreeland, W.N., Locascio, L.E., Using bioinspired thermally triggered liposomes for high-efficiency mixing and reagent delivery in microfluidic devices. Anal. Chem. 2003, 75, 6906-6911. [Pg.432]

Reagent delivery It is possible to add reagents to the sample while the experiment is running using the APTAC instrument. [Pg.933]

The Reaction Vessel Enclosure stores solvents and common reagents in 250-mL to 4-L bottles. Reagent delivery is mediated by a valve system. The accuracy of delivery is under the control of optical sensors. The autosampler handles up to 176 different reagents. The Reaction Vessel Enclosure contains 24 reaction vessels, which are organized in three banks of eight. [Pg.326]

MultiSynTech produces a manual version of its SYRO II synthesizer, SYRO II O. S. Manual Block. It does not have a robotic delivery system or a computer. Reaction blocks can be used just like with the SYRO II synthesizer. Reagent delivery is manual. All reaction parameters can be set up by a separate control unit. The Manual Block is substantially less expensive and less space consuming than its robotic equivalent. [Pg.334]

Figure 6.29 Details of a reagent delivery manifold in an inkjet microdispenser. Figure 6.29 Details of a reagent delivery manifold in an inkjet microdispenser.
This section discusses the most interesting acoustic levitation approaches for use in analytical chemistry and describes devices for sample positioning in the Ievitator and reagent delivery, ultrasonic levitators and the coupling of acoustic levitators to detection and separation systems. Also, it discusses future prospects for acoustic levitation. [Pg.270]

As part of a periodic maintenance schedule, the volume of fluid dispensed by the pipeter should be quantitatively assessed to detect any restricted flow that might occur owing to blockage of the pipeter. If double-mounted slides are used, with the control tissue placed at the bottom of the slide, the technologist will be made aware of any insufficient reagent delivery. [Pg.395]

Including all design issues within the mathematical formulation may complicate the model excessively, potentially slowing the solution down by an order of magnitude. Measurement noise, controller sampling effects, and detailed reagent delivery characteristics all fall into this category. [Pg.351]

Precision studies can be performed under different conditions, and are strongly influenced by variables such as temperature, source and quality of reagents, reproducibility of reagent delivery, and instrumental noise. Therefore, if all precision studies are done in the same laboratory (intralaboratory study) higher precision is expected in comparison with interlaboratory studies, where several laboratories produce the data used to prepare the method precision profile. [Pg.329]

Inaccuracy and imprecision for delivery of specimens from pipettes should not exceed 1%, Similar performance is desired for reagent delivery. The accuracy of the pipetting must be verified periodically, and such checks are a key factor in assessing the quality of instrument performance (see Chapter 14). The accuracy and reproducibility of pipettes in automated instruments are checked in the same way as they are for pipettes in manual systems (see Chapter 1). [Pg.272]


See other pages where Reagents delivery is mentioned: [Pg.496]    [Pg.132]    [Pg.67]    [Pg.225]    [Pg.83]    [Pg.47]    [Pg.450]    [Pg.655]    [Pg.56]    [Pg.64]    [Pg.106]    [Pg.84]    [Pg.310]    [Pg.68]    [Pg.333]    [Pg.337]    [Pg.338]    [Pg.250]    [Pg.441]    [Pg.270]    [Pg.832]    [Pg.873]    [Pg.351]    [Pg.369]    [Pg.322]    [Pg.268]    [Pg.274]    [Pg.190]   
See also in sourсe #XX -- [ Pg.274 ]

See also in sourсe #XX -- [ Pg.312 ]

See also in sourсe #XX -- [ Pg.500 ]




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Reagent delivery systems

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